Targeted disruption of TC-PTP in the proliferative compartment augments STAT3 and AKT signaling and skin tumor development

Tyrosine phosphorylation is a vital mechanism that contributes to skin carcinogenesis. It is regulated by the counter-activities of protein tyrosine kinases (PTKs) and protein tyrosine phosphatases (PTPs). Here, we report the critical role of T-cell protein tyrosine phosphatase (TC-PTP), encoded by Ptpn2, in chemically-induced skin carcinogenesis via the negative regulation of STAT3 and AKT signaling. Using epidermal specific TC-PTP knockout (K14Cre.Ptpn2fl/fl) mice, we demonstrate loss of TC-PTP led to a desensitization to tumor initiator 7,12-dimethylbenz[a]anthracene (DMBA)-induced apoptosis both in vivo epidermis and in vitro keratinocytes. TC-PTP deficiency also resulted in a significant increase in epidermal thickness and hyperproliferation following exposure to the tumor promoter, 12-O-tetradecanoylphorbol-13-acetate (TPA). Western blot analysis showed that both phosphorylated STAT3 and phosphorylated AKT expressions were significantly increased in epidermis of TC-PTP-deficient mice compared to control mice following TPA treatment. Inhibition of STAT3 or AKT reversed the effects of TC-PTP deficiency on apoptosis and proliferation. Finally, TC-PTP knockout mice showed a shortened latency of tumorigenesis and significantly increased numbers of tumors during two-stage skin carcinogenesis. Our findings reveal that TC-PTP has potential as a novel target for the prevention of skin cancer through its role in the regulation of STAT3 and AKT signaling.

signaling and POMC expression in the arcuate nucleus of the hypothalamus in response to insulin, suggesting that TC-PTP attenuates insulin signaling in POMC neurons 10 .
In regards to cancer, recent studies have shown that focal deletion of PTPN2 was detected in human T-cell acute lymphoblastic leukemia, implying TC-PTP has the potential to act as a tumor suppressor 11 . Studies also have shown that TC-PTP has a tumor suppressive function in breast and colorectal cancers mainly by regulating STAT3 signaling. The level of TC-PTP expression was decreased in a subset of breast cancer cell lines and a large proportion of triple-negative primary human breast cancers 12,13 . TC-PTP overexpression in human breast cancer cell lines suppressed cell proliferation and anchorage-independent growth with reduced tyrosine phosphorylation of STAT3 and SRC family kinase 12 . GdX (X-linked gene in the G6PD cluster at Xq28), which is known to act as a chaperon in protein processing in the endoplasmic reticulum, stabilizes the steady-state association of phosphorylated STAT3 with TC45 and promotes STAT3 dephosphorylation. Deletion of GdX in mice significantly accelerated colitis-associated colorectal tumorigenesis that corresponded with an increase in the level of phosphorylated STAT3 13 .
Initial studies of PTPs in skin showed that despite the fact that PTP expression is induced during keratinocyte proliferation and maturation, their expression levels remain unchanged within epidermal tissue 14 . Exposure to acute ultraviolet (UV) irradiation or treatment with the tumor promoter, 12-O-tetradecanoylphorbol-13-acetate (TPA), increases the activation of PTKs including the epidermal growth factor receptor (EGFR) and the downstream STAT3 signaling pathway [15][16][17][18][19][20] . One possible explanation for this result is that UV irradiation or TPA treatment induces PTP inactivation and in fact, studies revealed that reactive oxygen species produced by UV irradiation or TPA treatment triggered the inactivation of PTPs by oxidizing the cysteine residue within the conserved active-site of the PTP catalytic domain [21][22][23] . However, our recent studies showed that STAT3 is initially dephosphorylated in keratinocytes in response to UVB irradiation, and treatment with Na 3 VO 4 , a pan PTP inhibitor, recovered the level of phosphorylated STAT3 18 . Furthermore, our studies demonstrated that TC-PTP is one PTP that is responsible for UVB-mediated STAT3 dephosphorylation in skin 24 . UVB-mediated activation of TC-PTP resulted in a significant decrease in cell proliferation corresponding with a decrease of STAT3 phosphorylation in mouse keratinocytes 25 , suggesting that TC-PTP-mediated signaling may serve as part of a protective mechanism against skin carcinogenesis.
In the current study, we show a crucial role for TC-PTP in attenuating chemically-induced skin cancer formation. TPA initially increased STAT3 dephosphorylation and TC-PTP deficiency significantly reduced the effect of TPA on STAT3 dephosphorylation in mouse keratinocytes. In vivo studies using epidermal-specific TC-PTP knockout mice revealed that loss of TC-PTP significantly reduced 7,12-dimethylbenz[a]anthracene (DMBA)-induced apoptosis and increased TPA-induced cell proliferation mainly through the regulation of STAT3 and AKT phosphorylation, which resulted in enhanced skin cancer formation during DMBA/TPA skin carcinogenesis. These results suggest that TC-PTP plays a protective role against chemically-induced skin carcinogenesis.

Results
Knockdown of TC-PTP leads to reduced STAT3 dephosphorylation in mouse keratinocytes following TPA treatment. We previously showed that PTPs are involved in rapid STAT3 dephosphorylation in keratinocytes in response to UVB exposure 24 . Of the three PTPs involved in UVB-mediated STAT3 dephosphorylation, TC-PTP has a major role in regulating STAT3 signaling and significantly suppresses keratinocyte survival and proliferation following UVB irradiation 25 . In the current studies, we examined whether treatment with TPA, a potent tumor promoter, can result in rapid dephosphorylation of STAT3 because STAT3 plays a critical role in chemically-induced skin carcinogenesis [26][27][28][29] . Furthermore, we examined whether TC-PTP is involved in this mechanism given that TC-PTP can regulate STAT3 signaling. As shown in Fig. 1A, the level of phosphorylated STAT3 in mouse keratinocytes was decreased in response to TPA treatment in a dose-dependent manner. To demonstrate PTP is involved in this response, keratinocytes were cultured with Na 3 VO 4 . The level of phosphorylated STAT3 increased with higher doses of Na 3 VO 4 (Fig. 1B). In addition, pretreatment with Na 3 VO 4 for 2 h before TPA exposure recovered the level of STAT3 phosphorylation that was inhibited by TPA (Fig. 1C). To examine whether TC-PTP specifically is involved in TPA-induced STAT3 dephosphorylation, TC-PTP was knocked down using siRNA before TPA treatment. As shown in Fig. 1D, the level of STAT3 phosphorylation after TPA treatment in control keratinocytes transiently transfected with scrambled siRNA was significantly reduced compared to untreated control. However, the level of STAT3 phosphorylation after TPA treatment in keratinocytes transiently transfected with Ptpn2-specific siRNA was not reduced compared to untreated Ptpn2-deficient keratinocytes, indicating that TC-PTP is involved in the regulation of STAT3 phosphorylation following TPA exposure. To further examine the effect of TPA on STAT3 dephosphorylation in keratinocytes, cells were treated with TPA for 1 h and then harvested at the indicated time (Fig. 1E). Following the one hour pulse treatment of TPA, the level of phosphorylated STAT3 rapidly decreased but then recovered at later time points (Fig. 1E), which is similar to the results previously observed in keratinocytes after exposure to a low dose of UVB 25 . However, the level of phosphorylated STAT3 in a stable TC-PTP-knockdown keratinocyte cell line was not reduced by pulse treatment of TPA (Fig. 1F). During the promotion stage of skin carcinogenesis, initiated cells undergo clonal expansion induced by repeated exposure to a tumor promoter, which eventually leads to the development of benign tumors. Therefore, we treated keratinocytes with TPA for 1 h and then treated cells again 3 h after initial exposure to test if TC-PTP can be reactivated by repeated TPA treatments. A single treatment of TPA initially reduced the expression of phosphorylated STAT3 in control keratinocytes but then expression recovered after 8 h. However, re-treatment of the control cells with TPA after 3 h decreased phosphorylated STAT3 again (Fig. 1G). Furthermore, the second treatment of TPA effectively decreased the level of phosphorylated STAT3 beyond that of a single TPA treatment. The same effect was not seen in TC-PTP-knockdown keratinocytes (Fig. 1G) TC-PTP plays a major role in the regulation of STAT3 in the cellular response to TPA exposure and this response can serve as one critical protective mechanism against aberrant STAT3 activation by an environmental toxin.
Generation of skin specific Ptpn2 conditional knockout mice. Early lethality of TC-PTP knockout mice (~3-5 weeks of age) makes it impossible to characterize the functional role of TC-PTP in carcinogenesis using this mouse model 7 . Therefore, for this study, we generated epidermal specific TC-PTP knockout mice to further elucidate the protective role TC-PTP may play in chemically-induced skin cancer formation. To generate our mouse model, we obtained 'Knockout (KO)-first allele' transgenic mice established on a C57BL/6 congenic background that carry a floxed Ptpn2 allele from the EUCOMM/IMPC. We bred these 'KO-first allele' mice with FLPe mice (obtained from The Jackson Laboratory) to delete the targeting cassette including the splice acceptor gene and reporter gene and derive "conditional" Ptpn2 mice. We also obtained K14Cre transgenic mice established on a C57BL/6 congenic background that express human keratin 14-conrolled Cre recombinase in the basal cell layer of the epidermis and hair follicles from The Jackson Laboratory. The C57BL/6 strain is not suitable for carcinogenesis studies because of its strong resistance to chemical carcinogens. The FVB/N strain, on the other hand, is highly sensitive to chemically-induced skin carcinogenesis in comparison to other strains, such as C57BL/N 30 . Therefore, we backcrossed both "conditional" Ptpn2 mice and K14Cre mice against wild-type mice of FVB/N background for at least 10 generations. Then, conditional Ptpn2 mice were bred with K14Cre mice to generate epidermal specific TC-PTP knockout (KO, K14Cre.Ptpn2 fl/fl ) mice ( Fig. 2A). These TC-PTP KO mice were identified by genotyping with primers specific for Ptpn2 wild-type allele and Ptpn2 floxed allele which produced a 485 bp PCR product or a 382 bp PCR product, respectively (Fig. 2B). Western blot and immuohistochemical analysis clearly showed that TC-PTP KO mice do not express TC-PTP in the epidermis in contrast to control (WT, K14Cre.Ptpn2 w/w ) mice (Fig. 2C,D). We also isolated protein from other tissues of TC-PTP KO mice and found TC-PTP was expressed normally in all other tissues except epidermis, demonstrating epidermal specific deletion of Ptpn2 by Cre recombinase (Fig. 2E).

TC-PTP deficiency increases resistance to apoptosis.
In chemically-induced skin carcinogenesis, DNA damage caused by a carcinogen, such as DMBA, can be repaired by cellular DNA repair mechanisms otherwise, apoptotic signaling may be activated as protection against propagation of aberrant, damaged cells. However, damaged cells can acquire a growth advantage through carcinogen-induced mutation(s) during tumor initiation, if they have escaped these protective mechanisms, and these cells can clonally expand as a result of selective pressure by repetitive exposure to a tumor promoter, such as TPA 31,32 . To investigate the effect of TC-PTP deficiency on DMBA-induced apoptosis, primary keratinocytes from both K14Cre.Ptpn2 w/w and K14Cre.Ptpn2 fl/fl mice were (E) Western blot analysis of TC-PTP in non-epidermal tissues from K14Cre.Ptpn2 fl/fl mice. Brain, heart, liver, lung, and stomach were collected from K14Cre.Ptpn2 fl/fl mice and total cell lysates were prepared. cultured and treated with DMBA. As shown in Fig. 3A, there are no visible differences in morphology between TC-PTP WT and TC-PTP KO keratinocytes before DMBA treatment. However, 24 h after DMBA treatment, profound morphological changes induced by apoptosis, such as cell ballooning and bleb formation, were observed in control keratinocytes and loss of TC-PTP significantly reduced the apoptotic effect (Fig. 3A,B). Further analysis using flow cytometry showed that annexin V-positive cells were significantly increased wild-type keratinocytes compared to TC-PTP-deficient keratinocytes (Fig. 3C). Caspase-3 activity was also increased in wild-type primary keratinocytes following DMBA treatment whereas DMBA had little to no effect on caspase-3 activity in TC-PTP-deficient keratinocytes (Fig. 3D) as evidenced by the significant difference in activity between control and TC-PTP-deficient cells following treatment. Consistent with our in vitro results, the number of apoptotic cells, detected by active caspase-3 staining, within the epidermis of control mice was significantly increased compared to TC-PTP-deficient mouse epidermis 24 h after DMBA treatment (Fig. 3E,F). These results suggest that TC-PTP has a protective function in epidermis in that it mediates the removal of DNA-damaged keratinocytes following DMBA treatment.
Role of TC-PTP in TPA-induced epidermal hyperproliferation and hyperplasia. As previously mentioned, cells which survive the initiation stage confer a growth advantage and stimulate keratinocyte proliferation, resulting in epidermal hyperplasia during the tumor promotion stage. To investigate the effect of TC-PTP deficiency on TPA-induced keratinocyte proliferation and epidermal hyperplasia, primary keratinocytes derived from K14Cre.Ptpn2 w/w and K14Cre.Ptpn2 fl/fl mice were cultured. Interestingly, TC-PTP-deficient keratinocytes significantly grew faster (~1.5-fold, P < 0.05) than control keratinocytes (Fig. 4A,B). Following 1 h pulse treatment of TPA, keratinocytes from both genotypes exhibited an initial decrease in growth rate (Fig. 4C). After the short lag period, both keratinocytes began to grow again, but TC-PTP-deficient keratinocytes proliferated significantly faster (~3-fold, P < 0.05) than control keratinocytes.
To further investigate whether loss of TC-PTP confers a proliferative advantage in response to TPA on epidermal cells in vivo, both TC-PTP WT and TC-PTP KO mice were treated with TPA. As shown in Fig. 4D,E, there were no significant differences in the epidermal thickness of the two genotypes. However, application of TPA to the epidermis remarkably increased epidermal thickness in TC-PTP KO mice compared to control mice 24 and 48 h after treatment. BrdU labeling and PCNA staining, which measure active cell proliferation, showed a similar effect for TPA on epidermal thickness. Following TPA treatment, the number of either BrdU-positive or PCNA-positive cells in the epidermis of TC-PTP KO mice was significantly increased compared to control mice ( Fig. 4F-I). These results reveal that TC-PTP can play a role in protecting mouse epidermis against TPA-induced epidermal hyperproliferation.

Loss of TC-PTP confers higher proliferation and resistance against DMBA-induced apoptosis through STAT3 and AKT pathways.
We have shown previously and in our current study that TC-PTP dephosphorylates STAT3 (Fig. 1). EGFR is another substrate of TC-PTP that has a major role in cell growth 33 , consequently, TC-PTP negatively regulates PI3K/AKT and MAPK signaling pathways, which are downstream signaling pathways of EGFR 10,34-37 . Furthermore, these four signaling pathways -STAT3, EGFR, PI3K/AKT, and MAPK/ERK -are major pathways that are involved in skin carcinogenesis 38 . To investigate TC-PTP-mediated regulation of these signaling pathways during tumor promotion, both K14Cre.Ptpn2 w/w and K14Cre.Ptpn2 fl/fl mice were treated with TPA and epidermal cell lysates were prepared for western blot analysis. As shown in Fig. 5A, the level of phosphorylated STAT3 was higher in the epidermis of TC-PTP KO mice compared to that of control mice. In response to TPA treatment, the level of phosphorylated STAT3 was increased in both control and TC-PTP KO mice but the levels were higher in TC-PTP KO mice than control mice, especially 24 and 48 h after TPA treatment. The level of cyclin D1 expression, one critical target of STAT3, also was increased in both genotypes and its expression levels were higher in TC-PTP KO mice than control mice. However, the level of Bcl-xL expression was not changed in either genotypes following TPA treatment, indicating that Bcl-xL expression is independent of STAT3 and TC-PTP. Similar effects on Bcl-xL expression were observed in UVB-irradiated keratinocytes 24 . In addition, the level of phosphorylated EGFR was higher in TC-PTP KO mice than control mice in the absence or presence of TPA treatment. Similarly, the level of phosphorylated AKT was higher in TC-PTP KO mice compared to control mice with or without TPA treatment. The level of Bax expression, an apoptotic downstream target of AKT 39 , was also lower in TC-PTP KO mice compared to control mice. Interestingly, phosphorylated ERK1/2 was similarly expressed in both types of mice. We confirmed our in vivo results using primary keratinocytes derived from both genotypes (Fig. 5B). The levels of phosphorylated STAT3 and phosphorylated AKT were higher in TC-PTP-deficient keratinocytes compared to control keratinocytes with or without TPA treatment. The level of Mcl-1 expression, an anti-apoptotic downstream target of AKT 40,41 , was also higher in TC-PTP-deficient keratinocytes compared to control keratinocytes. TC-PTP deficiency has no effect on ERK1/2 phosphorylation in keratinocytes, as we observed with epidermis. To further examine whether TC-PTP-mediated regulation of STAT3 and AKT signaling has effects on DMBA-induced apoptosis, both wild-type and TC-PTP-deficient primary keratinocytes were treated with either a STAT3-specific inhibitor (S3I-201) or an AKT-specific inhibitor (A6730) before DMBA treatment. As shown in Fig. 6A and B, inhibition of STAT3 or AKT significantly increased cell sensitivity to DMBA-induced apoptosis in both control and TC-PTP-deficient keratinocytes, and the increased extent was higher in TC-PTP-deficient keratinocytes compared to control keratinocytes. In addition, DMBA-induced caspase-3 activity was significantly increased by inhibition of STAT3 or AKT in TC-PTP-deficient keratinocytes in comparison to DMBA-only control ( Fig. 6C; a,b,c). Interestingly, inhibition of STAT3 or AKT in TC-PTP-deficient keratinocytes could not completely recover the apoptotic effect of DMBA to the levels seen in wild-type keratinocytes (Fig. 6A-C), suggesting STAT3 and AKT have a synergistic effect and/or TC-PTP has an additional role(s) in DMBA-induced apoptosis. Additionally, we investigated the effects of STAT3 and AKT inhibition on TPA-induced keratinocyte proliferation. Both control and TC-PTP-deficient Scientific RepoRts | 7:45077 | DOI: 10.1038/srep45077  keratinocytes were treated with either STAT3 or AKT inhibitor before TPA treatment and then the number of cells were counted after seven days of TPA treatment. Inhibition of either STAT3 or AKT significantly decreased TPA-induced cell proliferation in TC-PTP-deficient keratinocytes compared to control keratinocytes ( Fig. 6D-F). Our results suggest that TC-PTP helps protect keratinocytes against tumor initiation and progression by facilitating DMBA-induced apoptosis and inhibiting TPA-induced cell proliferation via the negative regulation of STAT3 and AKT signaling.

Disruption of TC-PTP in epidermis significantly enhances skin tumor development.
To further demonstrate the protective role of TC-PTP during chemically-induced skin carcinogenesis, TC-PTP KO and control mice were subjected to a two-stage chemical carcinogenesis regimen. Both groups of mice were treated with DMBA. Two weeks after DMBA initiation, mice were treated with TPA twice weekly. TC-PTP KO mice were more sensitive to chemically-induced skin carcinogenesis in comparison to control mice (Fig. 7A-D). Even though 100% of both groups of mice developed papillomas by the end of experiments, TC-PTP KO mice developed papillomas faster than control mice. TC-PTP KO mice started to develop papilllomas 6 weeks after promotion, whereas control mice did not develop papillomas until 8 weeks after promotion. Even after 8 weeks, only 17% of the control group had developed papillomas while 100% of the TC-PTP KO group had already developed papillomas (Fig. 7B). Furthermore, the average number of papillomas/tumors per mouse was significantly greater (more than 2-fold) in TC-PTP KO mice compared with control mice (Fig. 7C). The average size of papillomas/tumors and the average number of carcinomas per mouse were also significantly greater in TC-PTP-deficient mice compared with control mice at the end of the experiments (Fig. 7D,E). Immunohistochemical and western blot analyses clearly showed that papillomas from control mice expressed TC-PTP, whereas papillomas from TC-PTP KO mice did not (Fig. 7H). In addition, papillomas from TC-PTP KO mice had significantly higher levels of phosphorylated STAT3 and phosphorylated AKT expression when compared with control ( Fig. 7F-H). Collectively, our findings indicate that TC-PTP mediates a protective mechanism that is able to attenuate chemically-induced skin carcinogenesis and its function is associated with the STAT3 and AKT signaling pathways.

Discussion
Phosphotyrosine-based signaling is regulated by the balanced actions of PTKs and PTPs, and it is involved in the regulation of various cellular processes including growth, differentiation, metabolism, and motility 42,43 . The aberrant activation of signaling pathways by mutation and/or overexpression of PTKs can lead to various types of cancers including skin cancer 44,45 . In this regard, PTKs have been considered to be attractive targets for cancer prevention and have been extensively studied in skin carcinogenesis. However, PTPs, the homeostatic counterpart of PTKs, have not been studied in skin carcinogenesis since environmental toxins, such as UV radiation or chemical toxicants, can cause PTP inactivation by attacking the conserved active site within the PTP catalytic domain through reactive oxygen species 22,23,46 . In the current study, we demonstrate for the first time that TC-PTP can play a role in the prevention of skin cancer formation induced by DMBA/TPA carcinogenesis regimen through the use of our epidermal specific TC-PTP knockout mouse model. Knockdown of TC-PTP in mouse keratinocytes significantly recovered the level of activated STAT3 that was reduced by treatment with TPA. We show that loss of TC-PTP promotes resistance to DMBA-induced apoptosis and TPA-induced hyperproliferation within  both in vitro primary keratinocytes and in vivo epidermis through the regulation of STAT3 and AKT signaling pathways. Furthermore, TC-PTP deficiency in epidermis significantly increased the number of papillomas/tumors and accelerated onset of tumor formation during two-stage skin carcinogenesis.
Previous studies showed that three PTPs -TC-PTP, SHP1, and SHP2 -cooperate to dephosphorylate STAT3 following UVB irradiation of mouse keratinocytes 24 . Further studies revealed that, of the three PTPs, TC-PTP is the major regulator of STAT3 signaling in keratinocytes during the response to UVB 25 . However, SHP1 and SHP2 may still contribute to STAT3 regulation or may be able to compensate for loss of TC-PTP. For instance, the previous studies demonstrated that following UVB exposure, levels of STAT3 phosphorylation in keratinocytes were quickly reduced but able to recover over time, with TC-PTP-knockdown cells expressing a higher level of active STAT3 compared to control; yet, even after recovery, the levels of phosphorylated STAT3 in TC-PTP-knockdown cells with and without UVB treatment were not the same. Also, the level of phosphorylated STAT3 after treatment with a low dose of UVB more rapidly recovered in TC-PTP-knockdown cells compared with control cells. In this study, we found that while the level of phosphorylated STAT3 was significantly decreased in control cells following TPA treatment, it was not decreased in TC-PTP-knockdown cells treated with TPA (Fig. 1D). Furthermore, TPA treatment did not induce a reduction of phosphorylated STAT3 in TC-PTP-knockdown cells, whereas it was initially decreased in similarly-treated control cells (Fig. 1F). These results suggest that the TPA-mediated mechanism of PTP activation is different from UVB. It is possible that either TPA activates only TC-PTP or it has a minimal effect on SHP1/SHP2 activation.
Our studies suggest that a single exposure to TPA does not constitutively activate TC-PTP. TC-PTP activation is reversible, as evidenced by the initial decrease and then recovery of phosphorylated STAT3 in keratinocytes after 1 h pulse treatment of TPA (Fig. 1F,G). However, re-treatment with TPA reduced phosphorylated STAT3 again, and this re-dephosphorylation of STAT3 was not observed in TC-PTP-knockdown cells, implying TC-PTP can be activated repeatedly by multiple applications of TPA (Fig. 1G). Our findings suggest that the reoccurring activation of TC-PTP during tumor promotion could continuously inhibit STAT3 phosphorylation/activation and thereby contribute to the prevention of skin cancer. It is the continuous activation of STAT3 by the repeated/ long-term exposure to TPA that contributes to the development of skin cancer. We found that a single treatment of TPA induced expression of phosphorylated STAT3, 24 and 48 hours after exposure in both TC-PTP WT and TC-PTP KO epidermis and primary keratinocytes and then expression of phosphorylated STAT3 decreased to basal levels. However, loss of TC-PTP resulted in a greater increase in phosphorylated STAT3 (Fig. 5A,B). Moreover, TC-PTP deficiency in primary keratinocytes prevented the decrease in phosphorylated STAT3 following TPA treatment (72 h, Fig. 5B). The results imply that TC-PTP is important in regulating STAT3 activation in response to TPA exposure and without TC-PTP, TPA would have a greater and more rapid effect on mouse epidermis. We show that TC-PTP-deficient mice develop papillomas more quickly than wild-type control mice and this result corresponds with an increase in phosphorylated STAT3 expression. Still, redundant and/or compensatory mechanisms to TC-PTP regulatory signaling may exist in epidermis to provide additional protection against environmental exposure as evidenced by the decrease in phosphorylated STAT3 72 h after TPA treatment in TC-PTP KO cells (Fig. 5A).
In addition to STAT3, AKT is another critical downstream target of PTK signaling in skin carcinogenesis [47][48][49][50] . Mouse models expressing either epidermal specific AKT or constitutively active AKT showed a significantly increased sensitivity to two-stage skin carcinogenesis 50 . Studies also have shown that TC-PTP negatively regulates AKT signaling. Gene copy loss of PTPN2 and lower mRNA levels in breast cancer was associated with AKT activation and poor prognosis 51 . Our studies showed that the levels of phosphorylated EGFR and phosphorylated AKT were constitutively higher in TC-PTP KO mice compared with control mice in the presence or absence of TPA treatment (Fig. 5A,B). Inhibition of AKT in TC-PTP-deficient keratinocytes significantly increased the sensitivity to DMBA-induced apoptosis and decreased cell proliferation induced by TPA ( Fig. 6A-C,F). Also, the level of phosphorylated AKT was higher in papillomas developed from TC-PTP KO mice during two-stage skin carcinogenesis (Fig. 7G,H).
In conclusion, use of our epidermal specific TC-PTP knockout mouse model provided evidence that TC-PTP can play a role in attenuating chemically-induced skin cancer formation through its continuous or prolonged activation. TC-PTP activation can lead to a significant increase in apoptosis induced by the carcinogen DMBA, and it facilitates the inhibition of cell proliferation mediated by tumor promoter TPA. TC-PTP performs these functions, mainly, by negatively regulating STAT3 and AKT signaling pathways. Our findings imply that modulation of TC-PTP regulatory signaling, which is not yet defined, and/or use of TC-PTP activators could contribute to the prevention of skin carcinogenesis. Overall, these studies suggest that TC-PTP activation may be a novel therapeutic strategy for the prevention and treatment of skin cancer. isolated from tail snips with three primers: CAS_R1_Term (TCGTGGTATCGTTATGCGCC), Ptpn2_47877_F (GCCAAGAGACAGTGGAAAGAGAG), Ptpn2_47877_R (ACTGCAAAACCATAACTGGC). Primers Ptpn2_47877_F and Cas_R1_term generate a 382 bp fragment corresponding to floxed Ptpn2 allele. Primers Ptpn2_47877_F and Ptpn2_47877_R generate a 485 bp fragment corresponding to wild-type Ptpn2 allele. Cre gene was also identified by polymerase chain reaction of genomic DNA. Female K14Cre.Ptpn2 fl/fl and K14CRE. Ptpn2 w/w littermates at 7-8 weeks of age were used for the described experiments. The dorsal skin of each mouse was shaved 48 h before treatment; only those mice in the resting phase of hair cycle were used. All animal handling procedures were approved by the Institutional Animal Care and Use Committee at University of Texas Rio Grande Valley and were in accordance with the NIH Guide for the Care and Use of Laboratory Animals.

Methods
Keratinocyte culture. 3PC keratinocytes (an immortalized mouse keratinocytes cell line obtained from Ca 2+ -resistant adult keratinocytes after DMBA exposure) 52 were obtained from University of Texas MD Anderson Cancer Center and cultured in low Ca 2+ (0.03 mM) EMEM (Lonza, #06-174 G) containing 5 ng/ml EGF, 2.5 μ g/ ml insulin, 5 μ g/ml hydrocortisone, 10 μ g/ml transferrin, 10 μ M ethanolamine, 10 μ M phosphoethanolamine, 1% penicillin/streptomycin and 1% fetal bovine serum at 37 °C and 5% CO 2 until 60 to 70% confluency at which time cells were treated with TPA. 3PC keratinocytes were verified by consistent morphological characteristic, with frozen aliquots from same passages (5 passages) used for experiments. Two day-old K14Cre.Ptpn2 fl/fl or K14Cre. Ptpn2 w/w neonates were used to culture primary keratinocytes as previously described 53 . Briefly, neonates were euthanized and skin was surgically removed. The skin was then placed in trypsin for 12 h at 4 °C to remove the dermis. Then, the isolated epidermis was minced and filtered by cell strainer (100 μ m) to get rid of debris. Primary keratinocytes were plated and cultured at 37 °C and 5% CO 2 in low Ca 2+ (0.03 mM) KGM-2 medium (Lonza, #CC-3158) containing 1% penicillin/streptomycin and 1% fetal bovine serum until 60 to 70% confluency at which time cells were treated with DMBA or TPA.
Knockdown of TC-PTP with siRNA and shRNA. 3PC cells were grown overnight to ~40% confluence and transfected with ON-TARGETplus TM mouse TC-PTP (Ptpn2) short interfering RNA (siRNA) and ON-TARGETplus TM siCONTROL ® Non-Targeting pool siRNA as control (Thermo Scientific Dharmacon). Transfection was performed with Lipofectamine ® RNAiMAX (Invitrogen) according to the manufacturer's instructions. TC-PTP-deficient stable cell lines established by lentiviral transduction with Ptpn2-specific shRNA were previously described 25 . Analysis of DMBA-induced apoptosis in primary keratinocytes and epidermis. Primary keratinocytes cultured from K14Cre.Ptpn2 w/w or K14Cre.Ptpn2 fl/fl neonates were treated with DMBA. Following incubation with DMBA for 24 h, keratinocytes presenting the morphological characteristics of apoptosis such as cell ballooning, nuclear condensation, and bleb formation were counted under phase contrast microscope. Apoptotic cells were counted from at least three non-overlapping fields. The percentage of apoptotic cells was calculated as follows: [number of apoptotic cells/(number of apoptotic cell plus number of viable cell)] × 100. To examine the effect of STAT3 or AKT on DMBA-induced apoptosis, keratinocytes were treated with STAT3 inhibitor S3I-201 (20 μ M, Selleck Chemicals) or AKT1/2 inhibitor A6730 (20 μ M, Sigma-Aldrich) 1 h before DMBA treatment. Capase-3 activity was measured by the caspase-3/CPP32 colorimetric assay kit (BioVision) according to the manufacturer's instructions.
To analyze DMBA-induced epidermal apoptosis, groups of K14Cre.Ptpn2 w/w and K14Cre.Ptpn2 fl/fl mice (n = 3/ group) were treated on the dorsal skin with a single topical application of DMBA (25 nmol) or acetone (200 μ l) and sacrificed 24 h after treatment. Skin sections were stained with an antibody to the active form of caspase-3 (R&D systems) and then treated with biotinylated anti-rabbit IgG-conjugated ABD reagent (BD Biosciences). Again, apoptotic keratinocytes were counted manually under phase contrast from at least 3 random, non-overlapping fields of view of tissue sections from 3 individual mice.

Flow cytometric analysis for apoptosis. Apoptosis of primary keratinocytes was evaluated using
Annexin V-FITC apoptosis kit (Molecular probe, V13242) according of the manufacturer's instructions. In brief, cells were harvested with 0.5% trypsin; 1 × 10 6 cells were then washed cold PBS and centrifuged at 400 × g for 5 min and stained using Annexin V-FITC. Then, cell suspensions were analyzed using LSRFortessa (BD Biosciences). The apoptotic rate was calculated as Annexin V-positive cells. Each experiment was performed three times, and data were presented as means ± SD.
Analysis of epidermal thickness and cell proliferation following TPA treatment. For analysis of epidermal thickness and proliferation, groups of 7 weeks old, female K14Cre.Ptpn2 w/w and K14Cre.Ptpn2 fl/fl mice (n = 3/group) were treated with a single topical application of TPA (6.8 nmol) or acetone on the dorsal skin and sacrificed 24 and 48 h after treatment. Thirty minutes prior to sacrifice, mice were injected intraperitoneally with 5-bromo-2-deoxyuridine (BrdU) (Sigma-Aldrich) in PBS at 100 μ g/g body weight. Dorsal skin was fixed in formalin and embedded in paraffin prior to sectioning at 4 μ m and then histological slides were stained with hematoxylin and eosin. Epidermal thickness was measured from 30 interfollicular sites per each group. To measure TPA-induced epidermal cell proliferation, sections were stained with an anti-BrdU antibody (BD Biosciences, #3263611), followed by treatment with biotinylated anti-mouse IgG and horseradish peroxidase-conjugated ABC reagent (Vector Laboratories). Epidermal cell proliferation, presented as the labeling index, was quantified by calculating the percentage of basal cells positive for BrdU. A minimum of 500 basal cells was counted. For immunofluorescence analysis of proliferating cell nuclear antigen (PCNA), sections were stained with an anti-PCNA antibody (Abcam, #ab29), followed by incubation with secondary mouse Alexa Fluor ® 647 antibody (Invitrogen, #A21236). Sections were counterstained with 4,6-diamidino-2-phenylindole (DAPI) to highlight cell nuclei (Invitrogen, #R37606). The expression of PCNA in the epidermis was detected by the Leica DMI6000 B fluorescence microscope (Leica) at wavelengths of 405 and 633 nm. Two-stage skin carcinogenesis. Groups of 7 weeks old, female K14Cre.Ptpn2 w/w and K14Cre.Ptpn2 fl/fl littermates (n = 12/group) were initiated with 25 nmol of DMBA or acetone. Two weeks after initiation, mice received topical treatments with 6.8 nmol of TPA twice a week until the experiment was terminated. Tumor incidence (percentage of mice with papillomas) and tumor multiplicity (average number of papillomas per mouse) were determined weekly until multiplicity plateaued. Papillomas were measured at the end of the experiment by digital calipers and tumor surface was calculated. Carcinomas (average number of carcinomas per mouse) were also counted at the end of the experiment. Difference in tumor incidence and multiplicity were analyzed by the χ 2 test and the Mann-Whitney U test, respectively.